Issue 26, 2023

Site-selective and stereoselective transformations on p-quinols & p-quinamines

Abstract

The intermolecular transformation of simple substrates into highly functionalized scaffolds with multiple stereogenic centers is an attractive strategy in modern organic synthesis. Prochiral 2,5-cyclohexadienones, being stable and easily accessible, are privileged key building blocks for the synthesis of complex molecules and bioactive natural products. In particular, p-quinols and p-quinamines are important subclasses of cyclohexadienones, having both nucleophilic and electrophilic sites, and can undergo various intermolecular cascade annulations via formal cycloadditions and other transformations. This article highlights the recent developments of intermolecular transformations on p-quinols and p-quinamines along with plausible reaction mechanisms. We hope that this review will inspire the readers to explore the new potential applications of these unique prochiral molecules.

Graphical abstract: Site-selective and stereoselective transformations on p-quinols & p-quinamines

Article information

Article type
Highlight
Submitted
03 Febr. 2023
Accepted
24 Febr. 2023
First published
25 Febr. 2023

Chem. Commun., 2023,59, 3795-3811

Site-selective and stereoselective transformations on p-quinols & p-quinamines

S. B. Thopate, M. Phanindrudu, S. B. Jadhav and R. Chegondi, Chem. Commun., 2023, 59, 3795 DOI: 10.1039/D3CC00509G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements